Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,380 recalls have been distributed to West Virginia in the last 12 months.
Showing 23121–23140 of 27,884 recalls
Recalled Item: Green Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...
The Issue: An investigation identified that high level friction may exist between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: These microcatheters were packaged with a 2.8 F distal tip, rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotome Biopsy Needle Set...
The Issue: MEDINVENTS, the manufacturer of the Spirotome" Soft-Tissue Biopsy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...
The Issue: The knife handles slot depth is out of specification, so blades may not fit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Moisture Last Multi-Purpose Solution Recalled by Bausch & Lomb Inc-...
The Issue: Product lot did not meet the specification for its disinfectants at the time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Recalled by...
The Issue: The insulin pump may lose time and date settings during a power interruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...
The Issue: Internal testing has confirmed a low absorbance range between the levels 1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant 04.1 mm RC Recalled by Straumann USA, LLC Due...
The Issue: Product transfer piece was fitted with a Narrow Connect (NC) instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...
The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety...
The Issue: An investigation identified that the product was incorrectly manufactured as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: Philips Allura Xper Systems...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...
The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...
The Issue: There is a potential for unintended and erratic motion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.